A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051972



Internal ID20619012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15328007..15353703hg38UCSC Ensembl
chr1:15654503..15680199hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3825697
hg1925697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322860
Supporting Variants
Samples
Known GenesFHAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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